Pharmacovigilance Services Specialist – Drug Safety & PV Operations
Location: Bengaluru, India
Company: Accenture
Job Type: Full-Time
Job ID: AIOC-S01633370
Experience Required: 5–10 years (7–11 years preferred in Pharmacovigilance/Drug Safety)
Educational Qualification: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm)
Overview
Accenture is seeking experienced Pharmacovigilance professionals to join its Life Sciences R&D division as Pharmacovigilance Services Specialists. This role is designed for senior drug safety professionals with strong expertise in pharmacovigilance operations, case processing, and regulatory compliance. You will play a critical role in ensuring patient safety by monitoring, evaluating, and reporting adverse drug reactions while supporting global pharmaceutical clients.
Key Responsibilities
The role involves end-to-end pharmacovigilance case management, including case identification, data entry, MedDRA coding, case processing, submission, and follow-up activities for Individual Case Safety Reports (ICSRs). You will ensure all deliverables meet global regulatory standards and client-specific guidelines.
You will analyze safety data from multiple sources, including clinical trials, healthcare professionals, and post-marketing surveillance, to detect and assess adverse events. The position also requires ensuring compliance with international pharmacovigilance regulations and maintaining high-quality safety databases.
In addition, you will contribute to process improvements, solve moderately complex operational challenges, and may lead small teams or manage specific workstreams. Collaboration with internal stakeholders, clients, and cross-functional teams will be essential to drive successful project outcomes.
Core Functional Expertise
Candidates are expected to have strong experience in pharmacovigilance operations, including ICSR lifecycle management, drug safety surveillance, signal detection awareness, and regulatory reporting. Familiarity with global safety databases, MedDRA coding, and pharmacovigilance workflows is essential.
Required Skills and Competencies
Applicants should demonstrate strong analytical and problem-solving capabilities with the ability to handle complex safety cases. A clear understanding of global pharmacovigilance regulations and compliance requirements is critical.
Strong communication and stakeholder management skills are required, as the role involves interaction with internal teams and client stakeholders. The ability to adapt to evolving processes, manage priorities, and work in a fast-paced environment is essential.
Leadership and Work Environment
This role may involve managing small teams or leading specific deliverables, requiring an understanding of team goals and alignment with organizational strategy. You will work under moderate supervision while contributing to decision-making that impacts team performance and client outcomes.
The position may require working in rotational shifts based on project requirements.
Career Growth and Opportunities
Joining Accenture provides exposure to global pharmacovigilance projects, advanced technologies, and international regulatory frameworks. The organization offers structured career progression, continuous learning opportunities, and the ability to work with leading pharmaceutical and biotechnology companies worldwide.
This is an excellent opportunity for experienced drug safety professionals to advance their careers in pharmacovigilance operations, regulatory compliance, and global life sciences services.
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